West China Journal of Stomatology ›› 2017, Vol. 35 ›› Issue (6): 576-582.doi: 10.7518/hxkq.2017.06.003

• Orginal Article • Previous Articles     Next Articles

Effects of geranylgeranyltransferase Ⅰ gene silencing by RNA interference on the migration and invasion of tongue carcinoma

Zhenggang Chen1,2(), Shuren Wang3, Jinghua Li4, Jinhong Han5, Qimin Wang1, Lei Tong1, Wenjun Liu6, Fang Yang1, Qingyuan Guo1, Dawei Guo1, Ying Wang7,8()   

  1. 1. Dept. of Stomatology, Qingdao Municipal Hospital, Qingdao 266071, China
    2. Dept. of Oral and Maxillofacial Surgery, Shanghai Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200011, China
    3. Dept. of Stomatology, Jiaozhou People’s Hospital, Jiaozhou 266300, China
    4. Central Laboratory, Qingdao Municipal Hospital, Qingdao 266071, China
    5. Yantai Stomatological Hospital, Yantai 264008, China
    6. Dept. of Ear-nose-throat, Qingdao Municipal Hospital, Qingdao 266071, China
    7. Dept. of Stomatology, Fourth People’s Hospital of Jinan, Jinan 250031, China
    8. College of Stomatology, Weifang Medical University, Weifang 261021, China
  • Received:2016-12-17 Revised:2017-09-05 Online:2017-12-20 Published:2017-12-01
  • Supported by:
    Supported by: National Natural Science Foundation of China (81372908);Qingdao Municipal Commission of Health and Family Planning (2014-WJZD009, 2013-WSZD011).

Abstract:

Objective RNA interference was used to silence geranylgeranyltransferase Ⅰ(GGTase-Ⅰ) in vitro and to study the effect of GGTase-Ⅰ on the migration and invasion of tongue squamous cancer cells. Methods Three small interfering RNAs (siRNA) were designed according to the GGTase-Ⅰ sequence by Genebank and were transfected into tongue squamous cancer cells Cal-27 to knock down GGTase-Ⅰ expression. The tested cells were divided into three groups, as follows: the RNA-interfered groups (GGTase-Ⅰ siRNA1, GGTase-Ⅰ siRNA 2, GGTase-Ⅰ siRNA 3), a negative control group (disrupted by random sequence NC-siRNA), and a blank control group. GGTase-Ⅰ and RhoA gene expressions were examined by quantitative real-time polymerase chain reaction (qRT-PCR) and Western blot. The optimum interference group was screened by qRT-PCR and Western blot and was assigned as the experimental group. Matrix metalloproteinase (MMP)-2 and MMP-9 protein expressions were examined by Western blot. GTP-RhoA expression of protein was examined by GST-pull down. The migration and invasion abilities were analyzed by wound healing assay and Transwell motility assay. Results GGTase-Ⅰ mRNA and protein expression in Cal-27 decreased significantly after transfection of GGTase-I siRNA (P<0.05). No significant difference of RhoA gene expression was detected. MMP-2, MMP-9, and GTP-RhoA protein expressions decreased significantly (P<0.05). The migration and invasion abilities were inhibited (P<0.05). Conclusion To inhibit GGTase-Ⅰ expression, the migration and invasion abilities of tongue squa-mous cancer cells should also be inhibited. Further studies on GGTase-Ⅰ may provide novel effective molecular targets for tongue squamous cancer cells.

Key words: geranylgeranyltransferase Ⅰ, RhoA, tongue squamous cancer, migration, invasion, matrix metallo-proteinase-2, matrix metalloproteinase-9

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